Abstract
The complete Currarino triad (or syndrome) consists of anorectal anomalies, a sacral bony defect, and a presacral mass. Generally autosomal dominant in its inheritance, incomplete penetrance also characterizes this syndrome. We report the case of a 12-day-old patient with vomiting in whom a diagnosis of incomplete Currarino syndrome was made.
MeSH terms
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Anal Canal / abnormalities*
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Anti-Bacterial Agents / therapeutic use
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Cardiac Output, Low / etiology
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Digestive System Abnormalities / complications
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Digestive System Abnormalities / diagnosis*
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Digestive System Abnormalities / genetics
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Dyspnea / etiology
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Emergencies
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Enterocolitis, Necrotizing / drug therapy
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Enterocolitis, Necrotizing / etiology
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Erythema / etiology
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Humans
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Hypoglycemia / etiology
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Ileostomy
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Infant, Newborn
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Magnetic Resonance Imaging
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Male
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Penetrance
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Rectum / abnormalities*
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Sacrum / abnormalities*
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Syringomyelia / complications
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Syringomyelia / diagnosis*
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Syringomyelia / genetics
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Tachycardia / etiology
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Vomiting / etiology*